Effect of Sodium Benzenesulfonate on SO42− Removal from Water by Polypyrrole-Modified Activated Carbon

Sodium benzenesulfonate was doped into polypyrrole-modified granular activated carbon (pyrrole-FeCl3·(6H2O)-sodium benzenesulfonate-granular activated carbon; PFB-GAC) with the goal of improving the modified GAC’s ability to adsorb sulfate from aqueous solutions. At a GAC dosage of 2.5 g and a pyrrole concentration of 1 mol L−1, the adsorption capacity of PFB-GAC prepared using a pyrrole:FeCl3·(6H2O):sodium benzenesulfonate ratio of 1000 : 1500 : 1 reached 23.05 mg g−1, which was eight times higher than that for GAC and two times higher than that for polypyrrole-modified GAC without sodium benzenesulfonate. Adsorption was favored under acidic conditions and high initial sulfate concentrations. Doping with sodium benzenesulfonate facilitated polymerization to give polypyrrole. Sodium benzenesulfonate introduced more imino groups to the polypyrrole coating, and the N+ sites improved ion exchange of Cl− and SO42− and increased the adsorption capacity of sulfate. Adsorption to the PFB-GAC followed pseudo-second-order kinetics. The adsorption isotherm conformed to the Langmuir model, and adsorption was exothermic. Regeneration using a weak alkali (NH3·H2O), which released OH− slowly, caused less damage to the polypyrrole than using a strong alkali (NaOH) as the regeneration reagent. NH3·H2O at a concentration of 12 mol L−1 (with the same OH− concentration as 2 mol L−1 NaOH) released 85% of the sorbed sulfate in the first adsorption-desorption cycle, and the adsorption capacity remained >6 mg g−1after five adsorption-desorption cycles.

Zeolite Composite Nanofiber Mesh for Indoxyl Sulfate Adsorption toward Wearable Blood Purification Devices

A nanofiber mesh was prepared for the adsorption of indoxyl sulfate (IS), a toxin associated with chronic kidney disease. Removing IS is highly demanded for efficient blood purification. The objective of this study is to develop a zeolite composite nanofiber mesh to remove IS efficiently. Eight zeolites with different properties were used for IS adsorption, where a zeolite with a pore size of 7 Å, H+ cations, and a silica to aluminum ratio of 240 mol/mol exhibited the highest adsorption capacity. This was primarily attributed to its suitable silica to aluminum ratio. The zeolites were incorporated in biocompatible poly (ethylene-co-vinyl alcohol) (EVOH) nanofibers, and a zeolite composite nanofiber mesh was successfully fabricated via electrospinning. The nanofiber mesh exhibited an IS adsorption capacity of 107 μg/g, while the adsorption capacity by zeolite increased from 208 μg/g in powder form to 386 μg/g when dispersed in the mesh. This also led to an increase in cell viability from 86% to 96%. These results demonstrated that this zeolite composite nanofiber mesh can be safely and effectively applied in wearable blood purification devices.

Prominent role of sulfate reduction in robust sulfur retention in subtropical soil

Sulfur budgets in catchments indicated that about 80% of the deposited sulfur was retained in the subtropical soil, it alleviates the historical acidification caused by elevated deposition. The strong sulfur retention was attributed to the reversible sulfate adsorption in previous studies. Here we report that sulfate reduction is a prominent yet thus far overlooked mechanism for sulfur retention, based upon the comprehensive evidence of soil sulfur storage and multi-isotope within entire soil profile along a hydrological continuum in a typical subtropical catchment of China. Using a dual isotopic mass balance model, we determined that annual flux of reduction accounted for approximately 38% of sulfur retention, which was close to the proportion of reduced species in soil. Consequently, the release of sulfur legacy would be less serious with the decreasing sulfur deposition in China, compared to the projections only considering adsorption.

Efficient Sulfate Adsorption on Modified Adsorbents Prepared from Zea mays Stems

The effect of temperature on the sulfate adsorption capacity of adsorbents prepared from corn stalks (Zea mays) was evaluated. Two bioadsorbents were prepared from biomass: a biochar modified with H2SO4 with mass: volume ratio 1:1 (B 1:1), and cellulose modified with cetyl trimethyl ammonium chloride (CTAC). There were also determined thermodynamic parameters (ΔG°, ΔS° and ΔH°) and it was studied the adsorption kinetics and isotherm. At 25 °C was obtained the highest adsorption capacity of 16.4 and 7.4 mg/g with mass/volume ratio B 1:1 and modified corn (MC) respectively; it was observed an adverse effect of temperature increase on bioadsorbents’ performance. The thermodynamic parameters showed that the adsorption process is exothermic, not spontaneous, and it was given by chemisorption. Adsorption kinetics showed that equilibrium was reached at 420 min and that the pseudo-second-order model adjusted the experimental data with R2 > 0.98 and qe of 16.64 and 7.48 mg/g for B 1:1 as well as MC. The adsorption isotherm showed a good fit to Freundlich’s model when using B 1:1, whereas using MC as adsorbents the data was adjusted by Dubinin-Radushkevich’s model. Zea mays stems are an abundant agricultural residue and are a good source for the preparation of biochar type bioadsorbents as well as the extraction of cellulose, its use is recommended in the removal of sulfates in solution.

Sulfate Kinetics and Adsorption Studies on a Zeolite/Polyammonium Cation Composite for Environmental Remediation

Sulfide mineral mining produces highly sulfate-contaminated wastewater which needs to be treated before disposal. A composite material was made from natural zeolite (NZ) and Superfloc® SC-581, a polyammonium cationic polymer. The resulting modified zeolite (MZ) demonstrated improved capacity for sulfate abatement from wastewater compared to NZ. Above pH 4.0, MZ retained positive surface charge while NZ remained negative. The effect of the ionic strength on the adsorption process was evaluated. Sulfate adsorption capacity was assessed and revealed MZ to be superior to NZ in all cases. Adsorption kinetics reached equilibrium after 10–12 h, with MZ adsorption being twice that of NZ; data fitted a pseudo-second order kinetic model. Adsorption isotherms reflected the high capacity of MZ for sulfate adsorption with maximum of 3.1 mg g−1, while NZ only achieved 1.5 mg g−1. The process corresponds to heterogeneous partially reversible adsorption of ionic species over the solid adsorbent. Langmuir–Freundlich parameters revealed that adsorption over MZ corresponds to an interaction eight times stronger than that on NZ. The sulfate adsorption pattern changes with ionic strength. Taken together, the composite formed between natural zeolite and polyammonium represents an adsorbent that maintains the adsorption capacity of zeolite and proves suitable for anionic species removal. Further prospect considers the testing of the composite with other anionic pollutants (arsenate, phosphate, perchlorate, etc.)

Modular Chitosan-Based Adsorbents for Tunable Uptake of Sulfate from Water

The context of this study responds to the need for sorbent technology development to address the controlled removal of inorganic sulfate (SO42−) from saline water and the promising potential of chitosan as a carrier system for organosulfates in pharmaceutical and nutraceutical applications. This study aims to address the controlled removal of sulfate using chitosan as a sustainable biopolymer platform, where a modular synthetic approach was used for chitosan bead preparation that displays tunable sulfate uptake. The beads were prepared via phase-inversion synthesis, followed by cross-linking with glutaraldehyde, and impregnation of Ca2+ ions. The sulfate adsorption properties of the beads were studied at pH 5 and variable sulfate levels (50–1000 ppm), where beads with low cross-linking showed moderate sulfate uptake (35 mg/g), while cross-linked beads imbibed with Ca2+ had greater sulfate adsorption (140 mg/g). Bead stability, adsorption properties, and the point-of-zero charge (PZC) from 6.5 to 6.8 were found to depend on the cross-linking ratio and the presence of Ca2+. The beads were regenerated over multiple adsorption-desorption cycles to demonstrate the favorable uptake properties and bead stability. This study contributes to the development of chitosan-based adsorbent technology via a modular materials design strategy for the controlled removal of sulfate. The results of this study are relevant to diverse pharmaceutical and nutraceutical applications that range from the controlled removal of dextran sulfate from water to the controlled release of chondroitin sulfate.